Clearance Summary
SAFETY INJECTION PORT received FDA 510(k) clearance under submission number K903541, sponsored by Du-Call Miller Plastics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-09-14.
- Submission: K903541
- Applicant / Sponsor: Du-Call Miller Plastics, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 1990-09-14
Classification & Regulation
This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.